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A randomized prospective study Comparing C-mac D-blade, Airtraq, and Fiberoptic bronchoscope for intubating patients with anticipated difficult airway

A randomized prospective study Comparing C-mac D-blade, Airtraq, and Fiberoptic bronchoscope for intubating patients with anticipated difficult airway

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201605001589209
Enrollment
120
Registered
2016-04-15
Start date
2016-03-01
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory

Interventions

C-mac D-blade
Airtraq
fiberoptic group

Sponsors

hesham mohamed marouf
Lead Sponsor
Naglaa khalil yousef
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients will be included in the study if they will have a predicted difficult airway as assessed by the presence of at least one of the following clinical predictors: mouth opening (interincisor distance) < 3.5 cm; thyromental distance < 6 cm, Mallampati score ¿ 3, limited mobility at the atlanto-occipital joint (< 15 ¿ ), according to Bellhouse & Dore.7 Mallampatti grade will be determined with the patient maximally protruding his tongue with the head in full extension during sitting position.8 Interincisor distance will be measured with the patient in sitting position, and thyromental distance will be measured from inside of the mentum to the thyroid cartilage with the head in full extension.9

Exclusion criteria

Exclusion criteria: Exclusion criteria will include patients require a nasal intubation, have ASA physical status IV or V, younger than 18 yr, have respiratory tract pathology or coagulation disorders, or are at risk of regurgitation-aspiration (known hiatus hernia, esophageal reflux, or not fasted). Also, patients with anticipated impossible intubation will be excluded [as patients with a history of impossible intubation, mouth opening (interincisor distance) less than 20 mm, or cervical spine fixed in flexion 14].

Design outcomes

Primary

MeasureTime frame
Time to tracheal intubation

Secondary

MeasureTime frame
Time required to visualize the vocal cords;The number of intubation attempts;The number of successful trial;- Complications;- Mean arterial blood pressure, heart rate and oxygen saturation;- Lowest O2 saturation

Countries

Egypt

Contacts

Public Contacthesham marouf

associate professor

heshammarouf@hotmail.com00201274366808

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026